Rapid Stratification of ARDS Patients
Using Randox Patented Biochip Technology
Rapid Stratification of ARDS Patients for Effective Treatment Plan Implementation
The Randox ARDS assay is a quantitative IL-6 & sTNFR1 immunoassay for use on the Evidence MultiSTAT analyser with a preparation time of 30 minutes and a run time of 36 minutes.
The data, when combined with additional clinical data, and analysed using a parsimonious statistical model, developed and operated by UCSF, aims to stratify ARDS patients into one of two inflammatory phenotypes. This is one of the aims of the prospective clinical trial (PHIND Study) the biochip is currently being used in.
Interleukin 6 (IL-6) is a soluble mediator with a pleiotropic effect on inflammation, immune response, and haematopoiesis. Although its expression is strictly controlled by transcriptional and post-transcriptional mechanism, dysregulated continual synthesis of IL-6 plays a pathological effect on chronic inflammation and autoimmunity.
Soluble tumour necrosis factor receptor-1 (sTNFR1) is a circulating form of their membrane bound counterparts (mTNFR1) which is essential for tumour necrosis factor alpha (TNFα)-signalling via different pathways. An interaction between both mTNFR1 and mTNFR2 leads to a proinflammatory stimulus via activation of nuclear factor kappa B (NF-κB) or activator protein 1 (AP-1), while mTHFR1 contains a death domain through which signalling leads to apoptosis.
Meet the Evidence MultiSTAT
The Evidence MultiSTAT is an easy to use, small footprint analyser facilitating on-site simultaneous detection of multiple biomarkers.
Using chemiluminescence as a measurement principle, the Evidence MultiSTAT consistently delivers accurate results.
As minimal sample preparation is required, quantitative results are provided in 36 minutes offering efficient and accurate ARDS stratification.
Meet the Cartridge
The Evidence MultiSTAT cartridge contains the reagents required for the chemiluminescent reaction to take place incorporated into its wells.
The process from sample entry to results can be completed in 2 simple steps, with minimal risk of human error.
No other components are required.
The product has been developed solely for use in the clinical trial and is currently marked for Investigational Use Only. Not for Diagnostic Purposes.
Want to know more?
Contact us or visit our Evidence MultiSTAT webpage.